Canonical Allele Identifier: CA619267412

Gene: FAH

Linked Data

• dbSNP Id: rs1332485450
• gnomAD v2: 15-80454855-C-T
• gnomAD v3: 15-80162513-C-T
• gnomAD v4: 15-80162513-C-T
• MyVariant Identifiers: chr15:g.80454855C>T (hg19) ; chr15:g.80162513C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80162513C>T , CM000677.2:g.80162513C>T	GRCh38
NC_000015.9:g.80454855C>T , CM000677.1:g.80454855C>T	GRCh37
NC_000015.8:g.78241910C>T	NCBI36
NG_012833.1:g.14515C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.*149C>T	ENSP00000507680.1:n.*149C>T
ENST00000682012.1:n.530+177C>T
ENST00000683593.1:n.2295C>T
ENST00000684363.1:c.486C>T	ENSP00000507314.1:n.486C>T
ENST00000684569.1:n.500+177C>T
ENST00000561421.6:c.455+177C>T MANE Select	ENSP00000453347.2:n.455+177C>T
ENST00000646551.1:n.1942+177C>T
ENST00000261755.9:c.455+177C>T	ENSP00000261755.5:n.455+177C>T
ENST00000407106.5:c.455+177C>T	ENSP00000385080.1:n.455+177C>T
ENST00000537726.5:n.778C>T
ENST00000539156.5:c.245+177C>T	ENSP00000454271.1:n.245+177C>T
ENST00000558022.5:c.455+177C>T	ENSP00000453152.1:n.455+177C>T
ENST00000558627.1:n.383+177C>T
ENST00000558767.5:n.893C>T
ENST00000561421.5:c.455+177C>T	ENSP00000453347.1:n.455+177C>T
NM_000137.2:c.455+177C>T	NP_000128.1:n.455+177C>T
XM_024449872.1:c.455+177C>T	XP_024305640.1:n.455+177C>T
NM_000137.4:c.455+177C>T MANE Select	NP_000128.1:n.455+177C>T
NM_001374377.1:c.455+177C>T	NP_001361306.1:n.455+177C>T
NM_001374380.1:c.455+177C>T	NP_001361309.1:n.455+177C>T